FDA applicant

Medix of Florida, Inc.

Walker, MI1 decision1983–19830 recalls

FDA records 1 decision for Medix of Florida, Inc. (Walker, MI) in 1983: 1 510(k) clearance. All are in product code BTI (Compressor, Air, Portable). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Medix of Florida, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medix of Florida, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medix of Florida, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Medix”

FDA records each applicant name separately; these may or may not be the same firm.

Medix Biotech, Inc. 39 Medix Medical Electronics (U.S.A.), Inc. 14 Medix I.C.S.A. 6 Medix Corp. 6 Medix Biochemica 1 Medix Pharmaceuticals Americas, Inc. 1

Medix of Florida, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medix”